Pure Global AI
ANVISA registration 81733730025Active

HEMOGLOBIN SUBTYPE

ANVISA Registration Number: 81733730025TRINITY BIOTECH DO BRASIL COMERCIO E IMPORTACAO LTDATRINITY BIOTECH PRIMUS CORPORATION DBA TRINITY BIOTECHRisk Class III
Verified
Device names
Technical name
HEMOGLOBIN SUBTYPE
View exact technical-name matches →
PT: HEMOGLOBINA SUBTIPO
Commercial name
FAMÍLIA A2+F CONTROLE E CALIBRADOR
View exact commercial-name matches →
Risk class
Class III
Registration details
Registration Number
81733730025
Process Number
25351137963202575
CNPJ
15648426000204
Company information
Registration Holder
TRINITY BIOTECH DO BRASIL COMERCIO E IMPORTACAO LTDA
Manufacturer
TRINITY BIOTECH PRIMUS CORPORATION DBA TRINITY BIOTECH
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Nov 24, 2025
Status
Active
About this record

Access comprehensive regulatory information for HEMOGLOBIN SUBTYPE in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81733730025 and manufactured by TRINITY BIOTECH PRIMUS CORPORATION DBA TRINITY BIOTECH. The registration is held by TRINITY BIOTECH DO BRASIL COMERCIO E IMPORTACAO LTDA with validity until Nov 24, 2035.

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.